Search results for Sirolimus

1471 hits were found for Sirolimus

# Family MCID Name MIFTS Score
1
P GRF003 Graft-Versus-Host Disease 71 11.841
2
ART140 Arteries, Anomalies of 52 11.750
3
LPP008 Lipoprotein Quantitative Trait Locus 65 11.665
4
LYM007 Lymphangioleiomyomatosis 68 8.950
5
PRT251 Proteinuria, Chronic Benign 58 8.300
6
c ACT135 Acute Graft Versus Host Disease 51 7.744
7
P TBR001 Tuberous Sclerosis 69 7.541
8
P KDN018 Kidney Disease 71 7.226
9
c TBR025 Tuberous Sclerosis 1 84 6.947
10
P MYC007 Myocardial Infarction 69 6.666
11
THR024 Thrombosis 56 6.617
12
P CRN300 Coronary Heart Disease 1 73 6.565
13
ISC004 Ischemia 61 6.432
14
SPN035 Spindle Cell Sarcoma 51 6.412
15
SRC014 Sarcoma 64 6.412
16
HMN016 Hemangioendothelioma 35 6.363
17
KPS004 Kaposi Sarcoma 76 6.248
18
HML018 Homologous Wasting Disease 21 6.132
19
END086 End Stage Renal Disease 54 6.052
20
c HYP836 Hypercholesterolemia, Familial, 1 73 5.760
21
CRN030 Coronary Stenosis 50 5.720
22
P THR014 Thrombocytopenia 66 5.674
23
c ACT075 Acute Myocardial Infarction 55 5.653
24
KPS002 Kaposiform Hemangioendothelioma 50 5.633
25
P LKM002 Leukemia 65 5.603
26
P NTR004 Neutropenia 62 5.341
27
MYL009 Myelodysplastic Syndrome 67 5.328
28
DFC004 Deficiency Anemia 74 5.242
29
P PLY014 Polycystic Kidney Disease 71 5.222
30
c HYP724 Hyperlipoproteinemia, Type Iii 66 5.136
31
P LYM118 Lymphoma 66 5.107
32
ANG054 Angina Pectoris 65 5.060
33
P SKN015 Skin Carcinoma 71 5.026
34
P LKM062 Leukemia, Acute Lymphoblastic 69 4.966
35
CRN020 Coronary Restenosis 39 4.915
36
P EXN002 Exanthem 58 4.874
37
c LKM061 Leukemia, Acute Myeloid 83 4.811
38
P VSC007 Vascular Disease 62 4.786
39
P HPT023 Hepatocellular Carcinoma 95 4.721
40
P HYP750 Hypertriglyceridemia, Familial 61 4.715
41
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 4.714
42
P UVT001 Uveitis 57 4.685
43
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 4.609
44
LYM022 Lymphangioma 54 4.596
45
INT007 Intermediate Coronary Syndrome 53 4.534
46
c CHR684 Chronic Kidney Disease 73 4.471
47
P DBT009 Diabetes Mellitus 67 4.463
48
P LYM033 Lymphoproliferative Syndrome 59 4.450
49
c CHR417 Chronic Graft Versus Host Disease 55 4.400
50
HYP056 Hypoglycemia 65 4.372
51
HMN047 Human Cytomegalovirus Infection 59 4.356
52
THR123 Thrombotic Microangiopathy 40 4.275
53
SFT003 Soft Tissue Sarcoma 43 4.158
54
LYM019 Lymphosarcoma 46 4.122
55
LPD008 Lipid Metabolism Disorder 61 4.076
56
LNG099 Lung Disease 62 4.057
57
P HMN010 Hemangioma 61 3.997
58
P MYL006 Myeloid Leukemia 60 3.989
59
P ANR048 Aniridia 1 66 3.969
60
LYM133 Lymphoma, Hodgkin, Classic 69 3.963
61
c TYP008 Type 1 Diabetes Mellitus 77 3.954
62
PST046 Post-Transplant Lymphoproliferative Disease 53 3.859
63
P LPS004 Lupus Erythematosus 61 3.750
64
LYM143 Lymphoma, Non-Hodgkin, Familial 74 3.709
65
MCS002 Mucositis 55 3.703
66
P HRT032 Heart Disease 84 3.666
67
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.626
68
c PST005 Posterior Uveitis 54 3.587
69
ANR040 Aneurysm 60 3.575
70
48X005 48,xyyy 39 3.563
71
ANG018 Angiomyolipoma 45 3.541
72
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.539
73
c SYS001 Systemic Lupus Erythematosus 85 3.482
75
P PNV001 Panuveitis 48 3.408
76
AND005 Androgen Insensitivity Syndrome, Mild 21 3.384
77
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.380
78
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.348
79
MYL005 Myelofibrosis 70 3.333
80
P GLM040 Glioma Susceptibility 1 70 3.326
81
ATH013 Atherosclerosis Susceptibility 63 3.311
82
P SCK005 Sickle Cell Disease 56 3.304
83
PRP027 Peripheral Vascular Disease 71 3.278
84
BRN002 Bronchiolitis 57 3.276
85
BRN012 Bronchiolitis Obliterans 56 3.272
86
HYP060 Hyperinsulinism 53 3.265
87
P NRF002 Neurofibromatosis 60 3.258
88
P APL001 Aplastic Anemia 72 3.246
89
P RRL003 Rare Lymphatic Malformation 31 3.236
90
ADL002 Adult Syndrome 69 3.199
91
RHB024 Rhabdomyosarcoma 2 65 3.188
92
LYM040 Lymphoblastic Lymphoma 53 3.180
93
P GLM007 Glomerulonephritis 59 3.175
94
c HPT001 Hepatitis C 61 3.162
95
BLR027 Blue Rubber Bleb Nevus 39 3.162
96
STM007 Stomatitis 52 3.150
97
GLB002 Glioblastoma 67 3.145
98
P MLG074 Malignant Mesenchymoma 40 3.116
99
P SRC025 Sarcoidosis 1 70 3.096
100
AGN016 Aging 53 3.092
101
HYP066 Hyperglycemia 60 3.089
102
P OVR082 Overgrowth Syndrome 41 3.087
103
OST159 Osteogenic Sarcoma 66 3.085
105
c CHR064 Chronic Monocytic Leukemia 35 3.082
106
MYL069 Myeloma, Multiple 76 3.080
107
P KDN017 Kidney Cancer 60 3.064
108
P TRN020 Turner Syndrome 67 3.061
109
P RSP003 Respiratory Failure 73 3.061
110
LYM005 Lymphocele 31 3.052
111
ART002 Arts Syndrome 66 3.049
112
P EYD002 Eye Disease 57 3.047
113
LMB062 Limb Ischemia 55 3.036
114
P FCL005 Focal Segmental Glomerulosclerosis 57 3.024
115
NRF007 Neurofibroma 63 3.013
116
HMN035 Hemangioma-Thrombocytopenia Syndrome 39 2.988
117
INT066 Interstitial Lung Disease 60 2.966
118
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.902
119
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 2.897
120
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 2.897
121
P HML002 Hemolytic Anemia 62 2.875
122
P HPT021 Hepatitis 68 2.861
123
c INT064 Intermediate Uveitis 54 2.855
124
c MCR115 Microvascular Complications of Diabetes 5 65 2.850
125
PLS009 Plasma Cell Neoplasm 64 2.825
126
P PRR002 Pure Red-Cell Aplasia 46 2.795
127
c ACT027 Acute Pancreatitis 60 2.793
128
c TYP009 Type 2 Diabetes Mellitus 91 2.788
129
P BRS047 Breast Cancer 97 2.771
130
P ACN011 Acne 55 2.766
131
IRN002 Iron Metabolism Disease 56 2.743
132
P LNG032 Lung Cancer 98 2.739
133
P PNC035 Pancreatic Cancer 87 2.712
134
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 2.699
135
P PNM007 Pneumonia 64 2.670
136
MCL006 Macular Retinal Edema 56 2.658
137
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 2.656
138
c MCR113 Microvascular Complications of Diabetes 3 52 2.649
139
KRT001 Keratoconjunctivitis Sicca 49 2.645
140
KRT006 Keratoconjunctivitis 53 2.645
141
P BCL017 B-Cell Lymphoma 57 2.628
142
MYL031 Myeloproliferative Neoplasm 66 2.613
143
c LKM063 Leukemia, Chronic Myeloid 70 2.602
144
JVN004 Juvenile Myelomonocytic Leukemia 66 2.589
145
c HRD202 Hereditary Lymphedema I 54 2.579
146
MLG169 Malignant Astrocytoma 57 2.557
147
P LVR013 Liver Disease 68 2.554
148
HMT002 Hematologic Cancer 61 2.551
149
KDN015 Kidney Angiomyolipoma 46 2.531
150
HGH043 High Grade Glioma 46 2.525
151
GLM045 Glioma 62 2.525
152
GLL048 Glial Tumor 51 2.525
153
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.516
154
P PNC044 Pancreatitis 61 2.486
155
c SML038 Small Cell Cancer of the Lung 68 2.449
156
ANT039 Antisynthetase Syndrome 55 2.448
157
BNM001 Bone Marrow Cancer 45 2.446
158
c ANM038 Anemia, Autoimmune Hemolytic 63 2.444
159
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 2.444
160
P ART005 Arteriovenous Malformation 64 2.410
161
DBT006 Diabetic Macular Edema 48 2.390
162
HMP001 Hemopericardium 47 2.380
163
P PRC012 Pericardial Effusion 50 2.380
164
CST005 Castleman Disease 56 2.363
165
MLT113 Multicentric Castleman Disease 46 2.363
166
P CRN074 Coronary Artery Aneurysm 41 2.335
167
P OVR042 Ovarian Cancer 88 2.320
168
ACR041 Acromelic Frontonasal Dysostosis 53 2.314
169
HYP005 Hypokalemia 55 2.313
170
P ENC018 Encephalopathy 62 2.306
171
CYT002 Cytokine Deficiency 43 2.285
172
CRH001 Crohn's Disease 80 2.282
173
PRP080 Peripheral Artery Disease 54 2.269
174
LNG031 Lung Benign Neoplasm 51 2.268
175
P DRR001 Diarrhea 55 2.255
176
P CNJ013 Conjunctivitis 66 2.254
177
P THL005 Thalassemia 56 2.254
178
STR039 Sturge-Weber Syndrome 60 2.246
179
WBR001 Weber Syndrome 38 2.246
180
PRV003 Perivascular Epithelioid Cell Tumor 38 2.243
181
CRN006 Coronary Aneurysm 41 2.241
182
P CHR285 Chronic Myelomonocytic Leukemia 59 2.235
183
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 2.235
184
c ACT073 Acute Leukemia 59 2.232
185
c CWD006 Cowden Syndrome 1 78 2.230
186
P MLN008 Melanoma 75 2.207
187
P ART021 Arteriosclerosis 53 2.205
188
SKN016 Skin Disease 63 2.196
189
MNT001 Mantle Cell Lymphoma 65 2.191
190
DWN001 Down Syndrome 70 2.190
191
CRD137 Cardiogenic Shock 56 2.188
192
HYP014 Hyperuricemia 51 2.157
193
P NPH012 Nephrotic Syndrome 61 2.145
194
HPT022 Hepatoblastoma 54 2.139
195
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 53 2.133
196
P LKM071 Leukemia, Chronic Lymphocytic 74 2.131
197
c ACT071 Acute Kidney Failure 60 2.131
198
CHL065 Cholangiocarcinoma 57 2.127
199
INT079 Intrahepatic Cholangiocarcinoma 51 2.127
200
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.123
201
P PRS040 Prostate Cancer 95 2.122
202
MLG077 Malignant Peripheral Nerve Sheath Tumor 53 2.116
203
c TBR026 Tuberous Sclerosis 2 71 2.107
204
PRP030 Purpura 54 2.103
205
IMM167 Immune Deficiency Disease 76 2.093
206
THY029 Thyroid Carcinoma 55 2.085
207
P TRM003 Tremor 50 2.083
208
P BLD134 Bladder Cancer 79 2.069
209
SQM006 Squamous Cell Carcinoma 59 2.067
210
c SPN330 Spondylocostal Dysostosis 5 55 2.063
211
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 2.054
212
HDG004 Hodgkin's Granuloma 22 2.042
213
HDG006 Hodgkin's Paragranuloma 22 2.042
214
c NRF024 Neurofibromatosis, Type I 76 2.040
215
PNC001 Pancytopenia 52 2.027
216
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.022
217
P RTN024 Retinoblastoma 72 2.019
218
P HML001 Hemolytic-Uremic Syndrome 52 1.998
219
CYS041 Cystic Angiomatosis of Bone, Diffuse 32 1.992
220
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 1.988
221
P INF037 Inflammatory Bowel Disease 53 1.987
222
GST045 Gastroenteritis 58 1.987
223
FBR054 Fibroma 44 1.980
224
EWN003 Ewing Sarcoma 69 1.980
225
c PRM038 Primary Agammaglobulinemia 47 1.967
226
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 1.963
227
SVR004 Severe Combined Immunodeficiency 70 1.963
228
P ADN016 Adenocarcinoma 63 1.962
229
P EPL164 Epilepsy 70 1.945
230
SKN013 Skin Benign Neoplasm 49 1.943
231
47X002 47,xyy 47 1.933
232
IRD001 Iridocyclitis 54 1.924
234
P PMP001 Pemphigus 54 1.923
235
c HPT073 Hepatitis C Virus 70 1.916
236
ACT003 Acute Kidney Tubular Necrosis 46 1.910
237
c ACQ016 Acquired Pure Red Cell Aplasia 29 1.909
238
P CWD010 Cowden Syndrome 70 1.902
239
PMP006 Pemphigus Vulgaris, Familial 57 1.897
240
c ACT068 Acute Cystitis 60 1.897
241
GLC003 Glucose Intolerance 53 1.894
242
P MDL005 Medulloblastoma 75 1.879
244
P VSC011 Vasculitis 61 1.878
245
CHR008 Choroiditis 48 1.873
246
IGG001 Iga Glomerulonephritis 50 1.863
247
P ESP024 Esophagitis 60 1.845
248
LYM027 Lymphopenia 56 1.835
249
P HYP050 Hyperinsulinemic Hypoglycemia 56 1.835
250
LYM095 Lymphangiomatosis 31 1.835
251
CNN005 Connective Tissue Disease 66 1.826
252
PNC129 Pancreatic Adenocarcinoma 64 1.823
253
PRT036 Peritonitis 65 1.823
254
P BNG030 Benign Ependymoma 51 1.806
255
CLL010 Cellular Ependymoma 58 1.806
256
P ADL010 Adult Respiratory Distress Syndrome 70 1.802
257
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.798
258
CRY001 Cryptogenic Organizing Pneumonia 53 1.794
259
P URN019 Urinary Tract Infection 48 1.785
260
PRL017 Prolymphocytic Leukemia 47 1.784
261
SPL004 Splenic Marginal Zone Lymphoma 50 1.783
262
CYS036 Cystinosis, Nephropathic 51 1.783
263
P PLM036 Pulmonary Fibrosis 65 1.780
264
END072 Endotheliitis 36 1.780
265
APH001 Aphthous Stomatitis 57 1.777
266
P NRB001 Neuroblastoma 66 1.775
267
P INF038 Influenza 68 1.767
268
P FML011 Familial Adenomatous Polyposis 70 1.757
269
c WLM013 Wilms Tumor 1 65 1.755
270
PHR003 Pharyngitis 57 1.736
271
CVD001 Covid-19 59 1.734
272
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.732
273
RHB001 Rhabdoid Cancer 68 1.732
274
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.730
275
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.724
276
ALL029 Allergic Disease 61 1.721
277
c BTT014 Beta-Thalassemia 72 1.716
278
P CMP005 Campomelic Dysplasia 65 1.715
279
P ANG015 Angioedema 56 1.704
280
SCK003 Sickle Cell Anemia 74 1.703
281
P EPN001 Ependymoblastoma 44 1.696
282
P CNR004 Cone-Rod Dystrophy 2 74 1.696
283
c MCR133 Microvascular Complications of Diabetes 4 41 1.683
284
c MCR130 Microvascular Complications of Diabetes 6 41 1.683
285
c MCR120 Microvascular Complications of Diabetes 7 47 1.683
286
P BNG032 Benign Mesothelioma 53 1.680
287
P SYS005 Systemic Scleroderma 73 1.680
288
P SJG008 Sjogren Syndrome 60 1.674
289
HPT046 Hepatic Veno-Occlusive Disease 54 1.667
290
LVR012 Liver Cirrhosis 62 1.666
291
BRN024 Bronchitis 67 1.662
292
P PLM006 Pulmonary Alveolar Proteinosis 53 1.659
293
CRN017 Coronary Thrombosis 46 1.655
294
HYP266 Hypoxia 56 1.655
295
c HYP595 Hypertension, Essential 84 1.650
296
P CLR023 Colorectal Cancer 100 1.641
297
PNM008 Pneumothorax 54 1.626
298
c ALP101 Alpha-Thalassemia 62 1.620
299
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.620
300
ACT011 Acute Contagious Conjunctivitis 41 1.620
301
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.620
302
SPR126 Superior Semicircular Canal Dehiscence 41 1.606
303
c HMG029 Hemoglobin Se Disease 41 1.606
304
P ANP001 Anaplastic Large Cell Lymphoma 59 1.603
305
GNG012 Gingival Overgrowth 49 1.600
306
GRM010 Germ Cells Tumors 33 1.600
307
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 1.600
308
P OVR046 Ovarian Cyst 43 1.599
309
HYP017 Hypophosphatemia 49 1.589
310
WLD007 Waldenstroem's Macroglobulinemia 59 1.575
311
LYM012 Lymphoplasmacytic Lymphoma 50 1.575
312
MCR004 Macroglobulinemia 48 1.575
313
c PCH015 Pachyonychia Congenita 1 60 1.574
314
P LPS002 Liposarcoma 64 1.574
315
INT002 Intermittent Claudication 61 1.560
316
ATM095 Autoimmune Disease 61 1.557
317
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.555
318
c HPT003 Hepatitis a 63 1.555
319
NRF003 Neurofibrosarcoma 43 1.555
320
SCH036 Scheie Syndrome 73 1.554
321
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 62 1.553
322
CHR563 Chronic Eosinophilic Leukemia 48 1.545
323
ATX019 Ataxia with Vitamin E Deficiency 44 1.545
324
P CHN012 Chondrosarcoma 56 1.543
325
P SCL015 Scleritis 47 1.543
326
c ANT023 Anterior Scleritis 30 1.543
327
P EPT020 Epithelioid Hemangioendothelioma 43 1.532
328
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 1.528
329
CRD001 Cardiac Tamponade 44 1.523
330
DRY001 Dry Eye Syndrome 49 1.507
331
KLP010 Klippel-Trenaunay-Weber Syndrome 59 1.504
332
FBR019 Fibromatosis 44 1.504
333
ASC009 Ascites, Chylous 31 1.497
334
STR067 Stroke, Ischemic 79 1.485
335
P RHM011 Rheumatoid Arthritis 81 1.476
336
SBP001 Subependymal Giant Cell Astrocytoma 45 1.476
337
P ART022 Arthritis 70 1.476
338
PRT013 Portal Hypertension 59 1.469
339
ALK024 Alkuraya-Kucinskas Syndrome 46 1.459
340
c ART144 Arthrogryposis, Distal, Type 1a 61 1.459
341
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.459
342
c SYS043 Systemic Lupus Erythematosus 1 38 1.459
343
PRS012 Pars Planitis 47 1.459
344
P DST002 Distal Arthrogryposis 63 1.459
345
CHR286 Chronic Neutrophilic Leukemia 42 1.459
346
CNT033 Central Nervous System Cancer 47 1.459
347
MXD026 Mixed Glioma 45 1.459
348
P PRP021 Peripheral Nervous System Neoplasm 39 1.459
349
P NRV006 Nervous System Cancer 47 1.459
350
P PRS038 Personality Disorder 65 1.459
351
CYT004 Cytomegalic Inclusion Disease 31 1.459
352
ACT250 Acute Megakaryocytic Leukemia 63 1.459
353
CNG506 Congenital Amyoplasia 27 1.459
354
P SZR006 Seizure Disorder 69 1.456
355
CYS002 Cystic Lymphangioma 45 1.449
356
IMP005 Impotence 52 1.438
357
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 1.432
358
MCL027 Macular Dystrophy, Dominant Cystoid 51 1.432
359
HYL004 Hyaline Fibromatosis Syndrome 67 1.432
360
ANG065 Angioma, Tufted 36 1.429
361
DFF031 Diffuse Alveolar Hemorrhage 31 1.418
362
HRP004 Herpes Zoster 60 1.415
363
P HMN032 Human Herpesvirus 8 47 1.412
364
P CYS018 Cystitis 58 1.412
365
DFF005 Diffuse Large B-Cell Lymphoma 55 1.402
366
c MYC058 Myocardial Infarction 2 23 1.396
367
c BSL007 Basal Cell Carcinoma 67 1.388
368
P PLY018 Polycythemia 56 1.386
369
PST011 Pustulosis of Palm and Sole 52 1.383
370
P PSR002 Psoriasis 63 1.383
371
SCT005 Scott Syndrome 51 1.381
372
CMM004 Common Variable Immunodeficiency 71 1.376
373
BRK010 Burkitt Lymphoma 65 1.366
374
KPS005 Kaposiform Lymphangiomatosis 24 1.365
375
P CTN015 Cutaneous T Cell Lymphoma 48 1.351
376
SVR001 Severe Acute Respiratory Syndrome 68 1.351
377
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 1.351
378
HMG005 Hemoglobinopathy 55 1.351
379
PTT041 Pituitary Stalk Interruption Syndrome 54 1.350
380
c PRS130 Prostate Cancer, Hereditary, 8 32 1.348
381
c PRS136 Prostate Cancer, Hereditary, 6 33 1.348
382
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 1.346
383
SKN019 Skin Melanoma 70 1.346
384
RFR002 Refractory Hairy Cell Leukemia 34 1.346
385
P NSP012 Nasopharyngeal Carcinoma 60 1.341
386
P EPD016 Epidermolysis Bullosa 53 1.341
387
PLX002 Plexiform Neurofibroma 44 1.341
388
BNR002 Bone Resorption Disease 47 1.335
389
CNG034 Congestive Heart Failure 69 1.335
390
P CRD246 Cardiovascular System Disease 55 1.328
391
P MYP004 Myopathy 67 1.314
392
ERD001 Erdheim-Chester Disease 53 1.292
393
c ATR087 Atrial Standstill 1 74 1.292
394
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.288
395
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 1.285
396
ATY042 Atypical Chronic Myeloid Leukemia 50 1.285
397
P ASP006 Aspergillosis 71 1.283
398
c HPT016 Hepatitis B 62 1.280
399
MCR141 Mucormycosis 59 1.280
400
P LMY004 Leiomyosarcoma 62 1.276
401
P ANT006 Antiphospholipid Syndrome 55 1.265
402
INV001 Invasive Aspergillosis 48 1.256
403
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.245
404
ERY051 Erythroleukemia, Familial 37 1.245
405
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 1.245
406
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 1.245
407
PRG023 Progeroid Short Stature with Pigmented Nevi 32 1.245
408
c OVR114 Ovarian Cancer 1 60 1.245
409
c LKM070 Leukemia, Acute Monocytic 56 1.245
410
c FNC043 Fanconi Anemia, Complementation Group E 62 1.245
411
PRT035 Peritoneum Cancer 45 1.245
412
CPL002 Capillary Lymphangioma 37 1.245
413
FLL027 Fallopian Tube Carcinoma 66 1.245
414
P EPD003 Epidermolysis Bullosa Simplex 56 1.245
415
P CCK001 Cockayne Syndrome 67 1.245
416
CHR682 Chronic Bilirubin Encephalopathy 37 1.245
417
ANP005 Anaplastic Astrocytoma 59 1.245
418
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.238
419
P GST053 Gastric Cancer 82 1.234
420
P LCH002 Lichen Planus 54 1.219
421
P RRT020 Rare Tumor 39 1.217
422
RNL077 Renal Fibrosis 46 1.206
423
MRK001 Merkel Cell Carcinoma 64 1.205
424
c LKM060 Leukemia, Acute Lymphoblastic 3 49 1.199
425
P BND020 Bone Disease 60 1.195
426
PRT018 Portal Vein Thrombosis 50 1.195
427
P RHB003 Rhabdomyosarcoma 66 1.194
428
CMB007 Combined Immunodeficiency 56 1.189
429
HST010 Histiocytosis 49 1.189
430
THR004 Thrombocytosis 52 1.188
431
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.188
432
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 1.188
433
INT020 Intravenous Leiomyomatosis 35 1.185
434
LMY003 Leiomyomatosis 43 1.185
435
P HYP086 Hypothyroidism 68 1.181
436
EVN001 Evans' Syndrome 46 1.173
437
INS001 Insulinoma 59 1.171
438
PRS047 Prostatitis 57 1.167
439
DYS073 Dysphagia 53 1.162
440
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 66 1.150
441
MSN004 Mesenchymal Cell Neoplasm 42 1.150
442
c ATM011 Autoimmune Hepatitis 62 1.138
443
CLL003 Cellulitis 53 1.138
444
EXP004 Exophthalmos 50 1.138
445
P PLY188 Polyendocrinopathy 29 1.138
446
P CYS039 Cystic Kidney Disease 52 1.134
447
PLY023 Polycystic Liver Disease 62 1.132
448
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.125
449
BKV001 Bk-Virus Nephropathy 23 1.125
450
P FNG006 Feingold Syndrome 1 61 1.113
451
ATX049 Ataxia with Vitamin 3 Deficiency 52 1.113
452
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 1.113
453
c BLD140 Blood Group, I System 47 1.113
454
c SCL052 Scleroderma, Familial Progressive 60 1.102
455
P MMB011 Membranous Nephropathy 50 1.102
456
NRR001 Neuroretinitis 42 1.102
457
KHN001 Kuhnt-Junius Degeneration 48 1.102
458
P RTN018 Retinal Disease 53 1.102
459
RTN023 Retinitis 45 1.102
460
RTR011 Retroperitoneal Fibrosis 47 1.102
461
CRB039 Cerebrovascular Disease 65 1.099
462
CRD132 Cardiac Conduction Defect 59 1.099
463
PLY179 Polyomavirus-Associated Nephropathy 25 1.098
464
HDR002 Hidradenitis Suppurativa 54 1.098
465
HDR003 Hidradenitis 49 1.098
466
c ACT134 Acute Liver Failure 57 1.098
467
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.098
468
KRT013 Keratolytic Winter Erythema 45 1.098
469
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 1.098
470
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 1.098
471
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 1.098
472
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.098
473
CHL068 Cholestasis 61 1.096
474
SPL018 Splenomegaly 47 1.086
475
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 1.086
476
IRN001 Iron Deficiency Anemia 58 1.069
477
CNS004 Constipation 56 1.069
478
CRH005 Crohn's Colitis 53 1.067
479
P INF032 Infertility 60 1.066
480
GST071 Gastrointestinal Carcinoma 46 1.062
481
P CPL006 Capillary Hemangioma 53 1.062
482
GST049 Gastrointestinal System Cancer 49 1.062
483
DSM004 Desmoid Tumor 65 1.062
484
P THY032 Thyroiditis 56 1.062
485
PNM001 Pneumocystosis 60 1.055
486
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 17 1.054
487
BRN028 Brain Cancer 73 1.052
488
P PLM037 Pulmonary Hypertension 69 1.038
489
INT067 Interstitial Nephritis 46 1.037
490
CRN019 Coronary Artery Vasospasm 47 1.037
491
FBR090 Fibro-Adipose Vascular Anomaly 16 1.037
492
P CHR012 Chronic Granulomatous Disease 69 1.036
493
c DWL002 Dowling-Degos Disease 1 58 1.020
494
CNT047 Contact Dermatitis 56 1.020
495
AMN001 Amenorrhea 53 1.010
496
MLG079 Malignant Pleural Mesothelioma 42 1.006
497
PLM033 Pulmonary Embolism 58 0.997
498
RRV005 Rare Vascular Tumor 17 0.997
499
P HYP077 Hypertrichosis 48 0.972
500
LFT001 Left Bundle Branch Hemiblock 47 0.972
501
GBM001 Gaba Aminotransferase Deficiency 31 0.966
502
P TRC086 Trichohepatoenteric Syndrome 1 59 0.966
503
CHN019 Chand Syndrome 31 0.966
504
P IGN003 Iga Nephropathy 1 39 0.966
505
CPL013 Capillary Malformations, Congenital 53 0.966
506
DSM003 Desmoid Disease, Hereditary 49 0.966
507
c FML346 Familial Adenomatous Polyposis 1 65 0.966
508
P HMN038 Human Coronavirus Sensitivity 30 0.966
509
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.966
510
BSL036 Basal Cell Nevus Syndrome 73 0.966
511
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.966
512
c HYP272 Hypercholesterolemia, Familial, 3 46 0.966
513
c FCL025 Focal Segmental Glomerulosclerosis 1 49 0.966
514
P SML001 Small Cell Carcinoma 52 0.966
515
MYX005 Myxoid Liposarcoma 65 0.966
516
AMD002 Amed Syndrome, Digenic 36 0.966
517
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.966
518
P MYS005 Myositis 55 0.966
519
INC002 Inclusion Body Myositis 56 0.966
520
MLT157 Multiple System Atrophy 1 69 0.966
521
c MST023 Mesothelioma, Malignant 56 0.966
522
FBR089 Fibrosclerosis, Multifocal 35 0.966
523
P ESP035 Esophagitis, Eosinophilic, 1 57 0.966
524
P ADL017 Adult T-Cell Leukemia 53 0.966
525
CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 35 0.966
526
LWG006 Low Grade Glioma 41 0.966
527
INT030 Intracranial Aneurysm 55 0.966
528
ACN001 Acinar Cell Carcinoma 44 0.966
529
IDP011 Idiopathic Interstitial Pneumonia 59 0.966
530
ACT029 Acute Interstitial Pneumonia 49 0.966
531
CRT016 Carotid Artery Disease 52 0.966
532
THY122 Thyroid Gland Cancer 59 0.966
533
ACD008 Acid-Labile Subunit Deficiency 52 0.966
534
DFF003 Diffuse Scleroderma 41 0.966
535
INT253 Intestinal Benign Neoplasm 46 0.966
536
NTR005 Nutritional Deficiency Disease 60 0.966
537
SML008 Small Intestine Lymphoma 33 0.966
538
GRM005 Germ Cell Cancer 46 0.966
539
P MSN005 Mesenchymal Chondrosarcoma 46 0.966
540
THY030 Thyroid Gland Disease 50 0.966
541
CLR017 Clear Cell Sarcoma 44 0.966
542
ESN005 Eosinophilic Gastroenteritis 55 0.966
543
GLS001 Gliosarcoma 63 0.966
544
ADL008 Adult Oligodendroglioma 35 0.966
545
CRB009 Cerebritis 43 0.966
546
BRN036 Brain Stem Infarction 38 0.966
547
FML008 Familial Retinoblastoma 49 0.966
548
P GRV001 Graves' Disease 54 0.966
549
MNT002 Mental Depression 56 0.966
550
HMG002 Hemoglobinuria 50 0.966
551
INT054 Intraocular Lymphoma 48 0.966
552
PNC015 Pancreatic Acinar Cell Adenocarcinoma 40 0.966
553
ACT118 Acute Non Lymphoblastic Leukemia 26 0.966
554
CYT018 Cytochrome P450 2d6 Variant 26 0.966
555
GST050 Gastrointestinal System Disease 55 0.966
556
c LKM005 Leukemia, T-Cell, Chronic 33 0.966
557
MTY003 Mutyh Polyposis 39 0.966
558
INT358 Intestinal Polyposis Syndrome 26 0.966
559
ACN026 Acinar Cell Carcinoma of Pancreas 28 0.966
560
IDP067 Idiopathic Hemiconvulsion-Hemiplegia Syndrome 20 0.966
561
PLS031 Plastic Bronchitis 26 0.966
562
c PRM369 Primary Acquired Pure Red Cell Aplasia 13 0.966
563
ANG062 Angioosteohypertrophic Syndrome 40 0.966
564
DPR016 Depression 64 0.966
565
CRB086 Cerebral Aneurysms 40 0.966
566
P OVR096 Overlap Myositis 27 0.966
567
c THR092 Thrombophilia Due to Thrombin Defect 74 0.958
568
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.953
569
CMB081 Combined Immunodeficiency, X-Linked 39 0.953
570
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.953
571
HMN044 Human Immunodeficiency Virus Type 1 76 0.953
572
ACQ007 Acquired Immunodeficiency Syndrome 58 0.949
573
BRT037 Brittle Diabetes 24 0.949
574
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.944
575
MDS022 Mediastinitis 47 0.944
576
P CHR345 Chronic Pain 50 0.944
577
PLM068 Pulmonary Vein Stenosis 39 0.929
578
ANG020 Angiosarcoma 63 0.926
579
PPL022 Papilloma 53 0.926
580
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.926
581
PNM010 Pneumothorax, Primary Spontaneous 58 0.913
582
DSS009 Disseminated Intravascular Coagulation 56 0.913
583
P HRP006 Herpes Simplex 65 0.913
584
PLS011 Plasmacytoma 56 0.909
585
P NJM001 Nijmegen Breakage Syndrome 75 0.907
586
c MGR028 Migraine with or Without Aura 1 63 0.900
587
PST028 Post-Traumatic Stress Disorder 58 0.900
588
TRN018 Transitional Cell Carcinoma 56 0.900
589
ADN018 Adenoma 58 0.900
590
VRT003 Vertebrobasilar Insufficiency 31 0.900
591
CLN015 Colon Adenocarcinoma 64 0.897
592
P OBS001 Obstructive Jaundice 49 0.897
593
PLY001 Polycythemia Vera 69 0.883
594
P URT039 Urticaria 57 0.879
595
EXT034 Extrinsic Allergic Alveolitis 56 0.879
596
LNG108 Langerhans Cell Histiocytosis 57 0.869
597
CHR072 Chordoma 56 0.869
598
ALC007 Alcohol Dependence 65 0.869
599
c ATM099 Autoimmune Uveitis 44 0.869
600
P NRP001 Neuropathy 59 0.869
601
BCT022 Bacterial Infectious Disease 55 0.865
602
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.860
603
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.860
604
FDL002 Food Allergy 47 0.860
605
c DLT002 Dilated Cardiomyopathy 79 0.860
606
RFR010 Refractory Anemia 49 0.844
607
INF013 Inferior Myocardial Infarction 33 0.840
608
P LPM005 Lipomatosis 47 0.840
609
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.840
610
NNN032 Non-Infectious Posterior Uveitis 18 0.840
611
c INF152 Infectious Posterior Uveitis 17 0.840
612
ISL001 Islet Cell Tumor 55 0.830
613
URM002 Uremia 47 0.827
614
P HYP098 Hypereosinophilic Syndrome 66 0.827
615
GTR002 Goiter 52 0.817
616
P RNL015 Renal Hypertension 45 0.817
617
CYS044 Cystic Disease of Lung 19 0.814
618
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.806
619
GNG013 Gingivitis 59 0.802
620
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.794
621
PRV023 Perivascular Epithelioid Cell Neoplasm 21 0.794
622
INT304 Interstitial Pneumonitis, Desquamative, Familial 42 0.791
623
RFL001 Reflex Sympathetic Dystrophy 51 0.791
624
ALG001 Algoneurodystrophy 37 0.791
625
ILS001 Ileus 49 0.791
626
RSD004 Rosai-Dorfman Disease 49 0.791
627
ADR016 Adrenal Cortical Carcinoma 61 0.789
628
P PYL005 Pyelonephritis 56 0.789
629
P ALP008 Alopecia 53 0.789
630
LYM035 Lymphangiectasis 30 0.789
631
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.783
632
P LTR001 Lateral Sclerosis 57 0.783
633
ORL013 Oral Lichen Planus 45 0.777
634
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.775
635
URT010 Ureteral Obstruction 44 0.775
636
ADR004 Adrenal Cortical Adenocarcinoma 38 0.775
637
HYD002 Hydronephrosis 58 0.775
638
ULC004 Ulcerative Colitis 74 0.775
639
PRP101 Peripheral Pulmonary Stenosis 24 0.770
640
CLT003 Colitis 63 0.761
641
FLL008 Folliculitis 45 0.761
642
P INT068 Intestinal Disease 53 0.761
643
P AGM001 Agammaglobulinemia 67 0.761
644
ACT058 Active Peptic Ulcer Disease 55 0.761
645
ANX004 Anoxia 40 0.761
646
P DRM010 Dermatomyositis 61 0.761
647
NPH018 Nephrogenic Systemic Fibrosis 48 0.761
648
JVN034 Juvenile Polyposis of Infancy 30 0.761
649
P PRK039 Parkinsonism 55 0.747
650
HMR023 Hemorrhagic Cystitis 43 0.747
651
SXL003 Sexual Disorder 49 0.746
652
TND005 Tendinitis 53 0.746
653
P SHR001 Short Bowel Syndrome 53 0.746
654
HPT019 Hepatic Encephalopathy 59 0.746
655
HPT004 Hepatic Coma 43 0.746
656
LMY002 Leiomyoma 51 0.743
657
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.743
658
FLL041 Follicular Lymphoma 1 44 0.743
659
P FLL037 Follicular Lymphoma 66 0.743
660
PLS016 Plasma Cell Leukemia 53 0.743
661
RTC005 Reticulosarcoma 47 0.743
662
P MXD050 Mixed Phenotype Acute Leukemia 46 0.743
663
P INS002 in Situ Carcinoma 52 0.733
664
ACT088 Acute Insulin Response 39 0.730
665
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.730
666
c BCT007 Bacterial Meningitis 55 0.730
667
ORL011 Oral Cancer 60 0.730
668
ANG037 Angiomatosis 31 0.730
669
ALL010 Allergic Contact Dermatitis 55 0.721
670
PSR001 Psoriatic Arthritis 61 0.714
671
c THR102 Thrombocytopenia 5 29 0.714
672
CLR109 Colorectal Adenocarcinoma 50 0.714
673
c VRL005 Viral Pneumonia 52 0.714
674
BLR008 Bilirubin Metabolic Disorder 57 0.714
675
BRN014 Bronchopneumonia 52 0.714
676
P END047 Endophthalmitis 53 0.714
677
ETV001 Etv6 Thrombocytopenia and Predisposition to Leukemia 31 0.714
678
APH002 Aphasia 55 0.707
679
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.707
680
ESP021 Esophageal Cancer 84 0.707
681
P LNG064 Lung Cancer Susceptibility 3 69 0.707
682
P FNC004 Fanconi Syndrome 60 0.707
683
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.696
684
GRN037 Granulomatosis with Polyangiitis 66 0.696
685
NCH001 Nuchal Bleb, Familial 25 0.696
686
ART004 Aortic Atherosclerosis 46 0.696
687
ART016 Aortic Aneurysm 68 0.696
688
ORL005 Oral Candidiasis 55 0.696
689
CPL003 Capillary Leak Syndrome 54 0.696
690
P CHL066 Cholangitis 51 0.696
691
c BCT013 Bacterial Pneumonia 47 0.696
692
GLM044 Glomerular Disease 34 0.696
693
LPM012 Lipomatosis, Multiple 59 0.677
694
IMM055 Immunodeficiency, Common Variable, 8, with Autoimmunity 42 0.677
695
OST003 Osteonecrosis 60 0.677
696
PLM005 Pleomorphic Lipoma 39 0.677
697
PRT019 Protein-Losing Enteropathy 44 0.677
698
KRT008 Keratopathy 46 0.677
699
P LRY044 Larynx Cancer 53 0.677
700
HMS001 Hemosiderosis 48 0.677
701
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.677
702
P ART023 Arthropathy 59 0.677
703
PLM010 Pulmonary Edema 54 0.677
704
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.677
705
AZS001 Azoospermia 45 0.677
706
CNT028 Central Retinal Artery Occlusion 42 0.677
707
TLN003 Telangiectasis 51 0.677
708
BRN026 Branch Retinal Artery Occlusion 41 0.677
709
SPC005 Speech Disorder 46 0.677
710
P RTN014 Retinal Artery Occlusion 46 0.677
711
P RTN016 Retinal Degeneration 52 0.677
712
ESN022 Eosinophilic Colitis 24 0.677
713
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.674
714
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 48 0.674
715
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.674
716
PLM070 Pulmonic Stenosis 49 0.674
717
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.674
718
PLM041 Pulmonary Valve Stenosis 50 0.674
719
MRT001 Muir-Torre Syndrome 59 0.657
720
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.657
721
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.657
722
P TMR010 Tumor Predisposition Syndrome 69 0.657
723
HYP080 Hypogonadism 49 0.657
724
P BRS053 Breast Fibroadenoma 48 0.657
725
P PLY019 Polyneuropathy 52 0.657
726
P LYN001 Lynch Syndrome 76 0.657
727
PDT021 Pediatric Osteosarcoma 34 0.657
728
NPH010 Nephrosclerosis 50 0.657
729
IRT001 Iritis 45 0.657
730
OLG001 Oligospermia 45 0.657
731
MYC021 Mycobacterium Xenopi 20 0.657
732
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.657
733
INH023 Inherited Cancer-Predisposing Syndrome 53 0.657
734
LGH007 Leigh Syndrome 70 0.647
735
PTZ001 Peutz-Jeghers Syndrome 69 0.647
736
P MLT020 Multiple Sclerosis 79 0.647
737
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.647
738
MSC007 Muscle Hypertrophy 64 0.647
739
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.647
740
LMY014 Leiomyoma, Uterine 55 0.647
741
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.647
742
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.647
743
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.647
744
RNL001 Renal Artery Obstruction 31 0.647
745
P MTR014 Motor Neuron Disease 65 0.647
746
MYF001 Myofibroma 42 0.647
747
NWB001 Newborn Respiratory Distress Syndrome 56 0.647
748
PDT045 Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcus Infections 24 0.647
749
RSP007 Respiratory Distress Syndrome, Infant 41 0.647
750
TCH005 Tièche-Jadassohn Nevus 28 0.647
751
P SCL018 Scoliosis 57 0.634
752
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.634
753
P CRD119 Cardiac Arrest 68 0.634
754
PHC018 Phace Association 37 0.634
755
RVL002 Ruvalcaba Syndrome 42 0.634
756
MCR037 Macroglossia 44 0.634
757
P BCK002 Beckwith-Wiedemann Syndrome 61 0.634
758
P LRY029 Laryngomalacia 47 0.634
759
MLT145 Multiple Enchondromatosis, Maffucci Type 49 0.634
760
PDT027 Pediatric Ulcerative Colitis 27 0.634
761
FML035 Familial Hyperlipidemia 54 0.634
762
VCC001 Vaccinia 49 0.634
763
P DMY001 Demyelinating Polyneuropathy 41 0.634
764
PLM001 Pulmonary Tuberculosis 69 0.634
765
VRN001 Vernal Conjunctivitis 35 0.634
766
MCR018 Microcytic Anemia 46 0.634
767
c MLG069 Malignant Hypertension 46 0.634
768
P RNL007 Renal Tubular Acidosis 52 0.634
769
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.634
770
BLP005 Blepharitis 50 0.634
771
HYG001 Hygroma Cervical 16 0.634
772
ORB014 Orbital Lymphangioma 23 0.634
773
EXT051 Extracranial Arteriovenous Malformation 26 0.634
774
CMP062 Complication After Organ Transplantation 10 0.634
775
RRV006 Rare Venous Malformation 8 0.634
776
ESN015 Eosinophilic Fasciitis 46 0.625
777
FSC004 Fasciitis 49 0.625
778
ACT119 Acute Promyelocytic Leukemia 62 0.611
780
P ATS364 Autism 72 0.611
781
c MCL013 Mucolipidosis Iv 64 0.611
782
c THR090 Thrombocythemia 1 50 0.611
783
TBC004 Tobacco Addiction 63 0.611
784
c FNC027 Fanconi Anemia, Complementation Group a 80 0.611
785
c GM1004 Gm1-Gangliosidosis, Type I 59 0.611
786
c GCH015 Gaucher Disease, Type I 67 0.611
787
c GCH016 Gaucher Disease, Type Ii 53 0.611
788
c GCH017 Gaucher Disease, Type Iii 52 0.611
789
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.611
790
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.611
791
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.611
792
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.611
793
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.611
794
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.611
795
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.611
796
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.611
797
ANG049 Angioedema Induced by Ace Inhibitors 38 0.611
798
PCK003 Pick Disease of Brain 70 0.611
799
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.611
800
FRN006 Frontotemporal Dementia 68 0.611
801
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.611
802
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.611
803
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.611
804
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.611
805
P PRK057 Parkinson Disease, Late-Onset 79 0.611
806
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 32 0.611
807
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.611
808
P KHL003 Kohlschutter-Tonz Syndrome 57 0.611
809
FCT007 Factor Vii Deficiency 64 0.611
810
GLS018 Glass Syndrome 60 0.611
811
P ESS003 Essential Thrombocythemia 68 0.611
812
P GCH001 Gaucher's Disease 69 0.611
813
P OLG002 Oligodendroglioma 66 0.611
814
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.611
815
PLS025 Plasmablastic Lymphoma 47 0.611
816
P DMN001 Diamond-Blackfan Anemia 73 0.611
817
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.611
818
c GM1007 Gm1 Gangliosidosis 65 0.611
819
VSL002 Visual Epilepsy 39 0.611
820
c PRM012 Primary Polycythemia 58 0.611
821
TNG007 Tongue Carcinoma 55 0.611
822
P DMN002 Dementia 65 0.611
823
c CNG027 Congenital Hemolytic Anemia 49 0.611
824
MYL003 Myeloid Sarcoma 48 0.611
825
CLR003 Clear Cell Adenocarcinoma 49 0.611
826
IND017 Indolent Plasma Cell Myeloma 41 0.611
827
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.611
828
GRN059 Grn Frontotemporal Dementia 16 0.611
829
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 0.611
830
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.611
832
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 37 0.611
833
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.611
834
CHL079 Children's Interstitial Lung Disease 25 0.611
835
LYS029 Lysosomal Disease 30 0.611
836
P GNG009 Gangliosidosis 44 0.611
837
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 0.611
838
TKY002 Takayasu Arteritis 61 0.608
839
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 52 0.608
840
P KBK002 Kabuki Syndrome 1 66 0.608
841
P MYS003 Myasthenia Gravis 67 0.608
842
PND002 Pendred Syndrome 57 0.608
843
P KLZ004 Kala-Azar 1 41 0.608
844
LMB024 Limbic Encephalitis 43 0.608
845
INT071 Intestinal Perforation 49 0.608
846
HMN004 Hemangioma of Liver 34 0.608
847
SMT002 Smooth Muscle Tumor 38 0.608
848
ACN003 Acneiform Dermatitis 37 0.608
849
P HYP061 Hypertrophic Cardiomyopathy 68 0.608
850
RNL011 Renal Osteodystrophy 48 0.608
851
P CTR002 Cataract 59 0.608
852
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.608
853
LSH001 Leishmaniasis 63 0.608
854
P MYC008 Myocarditis 59 0.608
855
P DST107 Distal Renal Tubular Acidosis 48 0.608
856
LYM051 Lymphomatoid Granulomatosis 44 0.608
857
ATN005 Autonomic Dysfunction 45 0.608
858
CLP006 Clopidogrel Resistance 44 0.608
859
PTR034 Paternal Uniparental Disomy 20 0.608
860
ABD010 Abdominal Wall Defect 37 0.608
861
MCR103 Microtia 40 0.608
862
P IDP049 Idiopathic Anterior Uveitis 36 0.608
863
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 44 0.578
864
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.578
865
WLS001 Wilson Disease 70 0.578
866
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.578
867
P JVN014 Juvenile Polyposis Syndrome 65 0.578
868
HMH004 Hemihyperplasia, Isolated 41 0.578
869
ACN002 Acanthosis Nigricans 56 0.578
870
c NPH049 Nephrotic Syndrome, Type 2 49 0.578
871
HMN048 Human Papillomavirus Infectious Disease 45 0.578
872
P MGR003 Migraine with Aura 51 0.578
873
P PRM002 Primary Hyperoxaluria 65 0.578
874
VSC006 Vascular Cancer 46 0.578
875
TRC005 Tracheal Stenosis 43 0.578
876
P OPT006 Optic Nerve Disease 57 0.578
877
c FML021 Familial Hypercholesterolemia 71 0.578
878
DRM006 Dermatitis 61 0.578
879
ANG016 Angiokeratoma 37 0.578
880
GST027 Gastric Lymphoma 43 0.578
881
CLF001 Cleft Lip 54 0.578
883
MCR088 Microscopic Polyangiitis 51 0.578
884
ARG006 Aregenerative Anemia 28 0.578
885
GNT019 Giant Cell Myocarditis 29 0.578
886
P HDC001 Headache 56 0.578
887
CLF004 Cleft Lip/palate 56 0.578
888
ATM106 Autoimmune Hemolytic Anemia, Cold Type 20 0.578
889
IDP091 Idiopathic Nephrotic Syndrome 49 0.578
890
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.538
891
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.538
892
NVS017 Nevus, Epidermal 66 0.538
893
AMN014 Aminopterin Syndrome Sine Aminopterin 31 0.538
894
HLC007 Helicobacter Pylori Infection 67 0.538
895
P MLT008 Multinodular Goiter 41 0.538
896
RTN004 Retinal Microaneurysm 32 0.538
897
GST023 Gastric Ulcer 52 0.538
898
CHR001 Churg-Strauss Syndrome 61 0.538
899
NNL001 Non-Langerhans-Cell Histiocytosis 35 0.538
900
P PLY011 Polycystic Ovary Syndrome 57 0.538
901
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.538
902
CDQ001 Cauda Equina Syndrome 37 0.538
903
CRT013 Carotid Stenosis 51 0.538
904
HST011 Histoplasmosis 54 0.538
905
RGH001 Right Bundle Branch Block 47 0.538
906
P ART018 Aortic Valve Insufficiency 52 0.538
907
SLN001 Silent Myocardial Infarction 33 0.538
908
ART012 Aortitis 41 0.538
909
AMR003 Amaurosis Fugax 32 0.538
910
ALL014 Allergic Encephalomyelitis 34 0.538
911
P HYP076 Hyperthyroidism 53 0.538
912
P SBR004 Seborrheic Dermatitis 44 0.538
913
GNT179 Genetic Steroid-Resistant Nephrotic Syndrome 40 0.538
914
ALL012 Allergic Angiitis 24 0.538
915
JVN033 Juvenile Nasopharyngeal Angiofibroma 45 0.538
916
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.527
917
c GLY008 Glycogen Storage Disease Ii 72 0.484
918
SQM002 Squamous Cell Papilloma 45 0.484
919
DSS032 Disease by Infectious Agent 55 0.458
920
GT001 Gout 63 0.458
921
MDD018 Middle East Respiratory Syndrome 44 0.451
922
HYP784 Hypogonadism, Male 43 0.442
923
PRP083 Porphyria, Acute Intermittent 64 0.442
924
c THR037 Thrombocytopenia 2 36 0.442
925
KWS002 Kawasaki Disease 65 0.442
926
c CHR708 Chronic Urticaria 42 0.442
927
PLM012 Pulmonary Sarcoidosis 52 0.442
928
P PRP029 Porphyria 60 0.442
929
TST015 Testicular Disease 42 0.442
930
MLT035 Multifocal Choroiditis 31 0.442
931
NDL013 Nodular Regenerative Hyperplasia 46 0.442
933
DFF020 Diffuse Idiopathic Pulmonary Neuroendocrine Cell Hyperplasia 17 0.442
934
ERS002 Erosive Pustular Dermatosis of the Scalp 22 0.442
935
PRQ002 Paraquat Poisoning 28 0.442
936
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.442
937
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.428
938
GST019 Gastrointestinal Stromal Tumor 78 0.428
939
END062 Endometrial Hyperplasia 47 0.428
940
c BSL024 Basal Cell Carcinoma 1 55 0.388
941
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.388
942
P ALZ034 Alzheimer Disease 87 0.388
943
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.388
944
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.388
945
END057 Endometrial Cancer 76 0.388
946
TCL003 T Cell Deficiency 44 0.388
947
BRR014 Barrett Esophagus 66 0.388
948
P RCT021 Rectum Cancer 54 0.388